Variant #0000277545 (NC_000005.9:g.140070876G>T, NM_012208.3:c.-358G>T (HARS2))
| Chromosome |
5 |
| Allele |
Unknown |
| Affects function (as reported) |
Does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.140070876G>T |
| DNA change (hg38) |
g.140691291G>T |
| Published as |
HARS(NM_001258040.1):c.14C>A (p.(Ala5Glu)), HARS(NM_002109.6):c.14C>A (p.A5E), HARS1(NM_002109.6):c.14C>A (p.A5E) |
| ISCN |
- |
| DB-ID |
HARS_000006 See all 4 reported entries |
| Variant remarks |
VKGL data sharing initiative Nederland |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
CLASSIFICATION record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.0054 View details |
| Owner |
VKGL-NL_AMC |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_AMC |
| Date created |
2018-01-15 20:58:59 +01:00 (CET) |
| Date last edited |
2024-08-28 13:16:32 +02:00 (CEST) |

Variant on transcripts
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